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Recalls affecting Nevada

Data last updated: September 7, 2026 at 12:15 AM UTC

16,425 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Mendietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc.Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Everything SproutsRobust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

MartinaMangoes

Potential contamination with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
Wording
Class IHigh risk
DrugUndeclaredRecalled August 27, 2015

MIRACLE DIET 30 capsules, 30-count bottle, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 7 538073516768.

Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain not listed on the label phenolphthalein, a drug product once contained in over-the-counter laxatives but was taken off the U.S. market due to safety concerns, making this product an unapproved drug.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0230-2016
Lot/product code:
All lots through Expiration Date 04/15/2018
Recalling firm:
The One Minute Miracle Inc
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled September 29, 2015

Amidate (Etomidate Injection, USP), 40 mg/20 mL (2 mg/mL), LifeShield, 20 mL, Glass Abboject Syringe with male luer lock adapter, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-8060-29

Failed Impurities/Degradation Specifications: not meeting quality requirements(OOS) results for degradation product of etomidate was confirmed during stability testing.

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0054-2016
Lot/product code:
Lot 34-531-DK, Exp 10/01/2015
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 1, 2015

The "Pacifier Activated Lullaby" (PAL) System composed of three major components: 1) the PAL Player Module (aka Player Unit), 2) the PAL Pacifier Sensor, and 3) power supply. The system is designed to encourage and reinforce effective non-nutritive sucking of premature infants.

PAL unit has undergone significant technological changes since the previous 510(k) and labeling is not consistent with the cleared indications of the 510(k).

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
72436
Lot/product code:
Serial Numbers A1221, A1226 (Ship Date 07/2015);   Serial Numbers A1061, A1250, A1251 (Ship Date 05/2015);   Serial Number A1246 (Ship Date 04/2015);   Serial Numbers A1245, A1244, A1042, A1243 (Ship Date 02/2015);   Serial Number A1225 (Ship Date 01/2015);   Serial Numbers A1241, A1242 (Ship Date 12/2014);   Serial Number A1036 (Ship Date 11/2014);   Serial Numbers A1229, A1247, A1224 (Ship Date 10/2014);   Serial Numbers A1239, A1234, A1236, A1237, A1238, A1233, A1228, A1231, A1232, A1235 (Ship Date 09/2014);   Serial Number A1227 (Ship Date 08/2014);   Serial Number A1223 (Ship Date 07/2014);   Serial Numbers A1218, A1220 (Ship Date 06/2014);   Serial Numbers A1217, A1216, A1248 (Ship Date 04/2014);   Serial Numbers A1214, A1064 (Ship Date 03/2014);   Serial Numbers A1087, A1213 (Ship Date 01/2014);   Serial Numbers A1201, A1203, A1204, A1205, A1206, A1209, A1210, A1211, A1212, A1094, A1200, A1207, A1091, A1092, A1093, A1201 (Ship Date 12/2013;   Serial Numbers A1075, A1076, A1077, A1078, A1079, A1080, A1081, A1082, A1083, A1070, A1072, A1073, A1084, A1086, A1087, A1088, A1089, A1090, A1085 (Ship Date 11/2013);   Serial Numbers A1022, A1044 (Ship Date 10/2013);   Serial Number A1059 (Ship Date 09/2013);   Serial Numbers A1021, A1060, A1062, A1063, A1065, A1066, A1067, A1069 (Ship Date 08/2013);   Serial Numbers A1037, A1005, A1015, A1024, A1230, A1050, A1051, A1052, A1053, A1054, A1055, A1058, A1016, A1019, A1064, A1249 (Ship Date 07/2013);   Serial Numbers A1006, A1020, A1004, A1023, A1021 (Ship Date 05/2013);   Serial Numbers A1025, A1046, A1032 (Ship Date 04/2013);   Serial Numbers A1038, A1049, A1029, A1026, A1035, A1039, A1036, A1031, A1030, A1028, A1027, A1034 (Ship Date 03/2013);   Serial Number P11 (Ship Date 02/2013);   Serial Number P-7 (Ship Date 11/2012);   Serial Numbers A1013, P-8 (Ship Date 09/2012);   Serial Numbers A1043, P-6, A1041, P-9 (Ship Date 07/2012);
Recalling firm:
Powers Medical Devices, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 2, 2015

Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5

The firm has received 15 complaints over ten years related to the connection of the spring arm to the top horizontal arm of the lighting system that while positioning the light head enabled the spring arm and light head to fall.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
72542
Lot/product code:
4028110 - iLED Single; 4028210 - iLED duo; 4028310 - iLED trio/quad; 4038110 - TruLight single; 4038210 - TruLight duo; 4038310 - TruLight trio/quad; 1565068 - iLED single (TUSM); 1565160 - iLED duo (TUSM); 1565161 - iLED trio/quad (TUSM); 1574759 - TruLight single (TUSM); 1574850 - TruLight duo (TUSM); 1574851 - TruLight trio/quad (TUSM)
Recalling firm:
Trumpf Medical Systems, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled December 3, 2015

Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion 3010 and 3010A Syringe Infusion Pumps serviced during the same time period in which a main board was replaced using replacement main board part numbers G6000361, G6000435, G6001260, G6001560, G6001562 and G6002728.

There have been intermittent issues with Supercap POST (power on self-test) and Backup Audible Alarm error codes outside of the pump warranty period. These alarms occur at start up when the pump goes through the self-test. This recall occurred in 2015.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
89144
Lot/product code:
Medfusion 3500 and 4000 Syringe Infusion Pumps manufactured between April 2012 and June 2015; and Medfusion 3010 and 3010A (and pump models 3500 and 40000 serviced during April 20121 and June 2015 in which a main board was replaced.
Recalling firm:
Smiths Medical ASD Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 23, 2015

APEXXX tablets, 300 mg, packaged in 1-count blister cards, Distributed Exclusively by: Nuway Distributors, LLC, Orlando, FL USA; UPC 7 05105 96361 7.

Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with sildenafil, an FDA approved drug for the treatment of male erectile dysfunction, making this an unapproved drug.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0667-2016
Lot/product code:
All lots
Recalling firm:
Nuway Distributors, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenUndeclaredRecalled January 20, 2016

Fruit Tartlets, Raspberry flavor, 9 - 0.56oz (16 g) tartlets - Net Wt. 5.1oz (145 g). Manufactured in France. Distributed by Ouhlala Gourmet Corp. dba Buddy Fruits, Coral Gables, FL

Products contain not listed on the label milk on finished product labeling

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-1420-2016
Lot/product code:
Lot Code (Exp date): 08212016 (08212016), 100116 (100116), 100122016 (100122016), 100216 (100216), 10302016 (10302016), 111316 (111316).
Recalling firm:
Ouhlala Gourmet Llc
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenUndeclaredRecalled January 20, 2016

Fruit Tartlets, lemon flavor, 9 - 0.53oz (15 g) tartlets - Net Wt. 4.8 oz (135 g). Manufactured in France. Distributed by Ouhlala Gourmet Corp. dba Buddy Fruits, Coral Gables, FL

Products contain not listed on the label milk on finished product labeling

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-1419-2016
Lot/product code:
Lot Code (Exp date): 08192016 (08192016), 09292016 (09292016), 10092015 (10092015), 10302016 (10302016), 10312016 (10312016), 111216 (111216), 10012016 (10012016), 09292016 (09292016), 10312016 (10312016). Item GTIN #00810387020566. Case UPC #20854417002430.
Recalling firm:
Ouhlala Gourmet Llc
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenUndeclaredRecalled February 1, 2016

Lysander's Premium Teriyaki Marinade, 1 oz (28 g), polypropylene and clamshell style card, 12 units per case. Manufactured by Geneva Foods, LLC.

Product contains not listed on the label allergens soy and wheat. Also does not declare sulfites.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2079-2016
Lot/product code:
Cases coded 2014-2015, if not visible all lots; UPC: 0-34795-00036-5.
Recalling firm:
Geneva Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenUndeclaredRecalled February 1, 2016

Lysander's All Natural Bourbon Flavor Rub; for beef, chicken, pork, and fish; 3.8 oz (107.7 g), foil bag, 6 units per case. Manufactured by Geneva Foods, LLC.

Product contains not listed on the label allergens soy and wheat. Also does not declare sulfites.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2081-2016
Lot/product code:
Lot codes ending in 14 or 15; UPC: 0-34795-00049-5.
Recalling firm:
Geneva Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenUndeclaredRecalled February 1, 2016

Lysander's All Natural Spicy Bourbon Flavor Rub; for beef, chicken, pork, and fish; 3.8 oz (107.7 g) foil bag, 6 units per case. Manufactured by Geneva Foods, LLC.

Product contains not listed on the label allergens soy and wheat. Also does not declare sulfites.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2080-2016
Lot/product code:
Lot codes ending in 14 or 15; UPC: 0-34795-00051-8
Recalling firm:
Geneva Foods, LLC
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled February 2, 2016

Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection Type 1, USP, 1000 mL Single-Dose Container bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7965-09, Barcode (01) 0 030409 796509 0.

Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer report of an incorrect expiration date printed on the primary container labeled "01AUG1017" rather than "01AUG2017".

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0727-2016
Lot/product code:
Lot #: 56-853-FW, Exp 01AUG2017
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 29, 2016

Medica ISE Module Calibrant A; 500 mL - 140 mmol/L Na+, 125 mmol/L Cl-, buffers and preservatives; For use with ISE Module; Product Usage: Calibrations of ISE Model for integrated electrolyte system analysis.

Lot was not functioning properly and not exhibiting the correct physical properties.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
77481
Lot/product code:
P/N 5409; Lot No. 15251; Exp. Date 09/2016
Recalling firm:
AMS Diagnostics, LLC
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled March 15, 2016

Quelicin (Succinylcholine Chloride) Injection, USP 200 mg. (20 mg/mL), 10 mL Multiple-dose vial, packaged in 25 Unit vials per carton, Rx only, HOSPIRA, INC., LAKE FOREST, IL 60045 USA, NDC 0409-6629-02

Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for the lot number and/or expiration date to be faded or missing from the primary label on the glass vial.

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0836-2016
Lot/product code:
Lot 52-045-EV, Exp 07/1/2016
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 18, 2016

8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest, IL 60045, NDC 0409-6625-02

Presence of Particulate Matter: particulate matter identified as an insect in one vial.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0865-2016
Lot/product code:
Lot # 56-148-EV, Exp 8/1/2017
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 23, 2016

Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.

Presence of Particulate Matter: Confirmed customer complaint for the presence of particulate matter.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1137-2016
Lot/product code:
Lot #: 50-343-DK*, Exp 01FEB2017; note that the lot number may be followed by numbers from 01 to 99.
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled March 23, 2016

Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.

Failed pH Specifications: Confirmed high not meeting quality requirements (OOS) results for pH.

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0854-2016
Lot/product code:
Lot #: 42-335-DK, Exp 1JUN2016; 48-128-DK, 48-129-DK, 48-261-DK, 48-262-DK, 48-351-DK, Exp 1DEC2016; 52-361-DK, Exp 1APR2017; note that the lot number may be followed by numbers from 01 to 99.
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled March 31, 2016

LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL

Marketed Without An Approved NDA/ANDA: Contains an unapproved drug, ligandrol LGD-4033

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0910-2016
Lot/product code:
Lot # 21511166, Exp 11/18
Recalling firm:
Invisiblu International LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled April 2, 2016

Human Chorionic Gonadotropin, 15,000 IU per vial, lyophilized for injection, Rx only, Complete Pharmacy & Medical Solutions, Miami Lakes, FL 33014

Non-sterility - presence of bacteria confirmed by outside laboratory after day 14.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0918-2017
Lot/product code:
Lot # 22016, Exp 1/30/2017
Recalling firm:
Complete Pharmacy and Medical Solutions LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 11, 2016

TRUE 3D VIEWER SYSTEM Model Number EP-00001-XX Software versions 1.0, 1.25, and 1.35 The t3D-Viewer is designed for use by health care professionals HCPs and is intended to assist the clinician who is responsible for making all patient management decisions. The True 3D Viewer (t3D-Viewer) system is comprised of a commercial off the shelf hardware platform and a proprietary software application that enables a health care professional (HCP) to visualize and interact with CT and MRI DICOM image data to assist in clinical decision making. The t3D-Viewer system hardware platform is comprised of an off the shelf stereoscopic display, an optical or electromagnetic motion tracking system and a computer system.

Imaging system data may be displayed with an incorrect orientation (sidedness) where the patient side is not correct (left, right, superior, inferior, anterior or posterior). This may lead to an inaccurate measurements.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
96629
Lot/product code:
Model Number EP-00001-XX with software versions 1.0, 1.25, and 1.35 UDI-DI Codes: 00851325007003 Serial Numbers: Field Products: C2015-09-0001 C2015-09-0003 D2015-05-0002 C2015-06-0002 D2015-12-0004 C2015-08-0001 D2015-12-0005 C2015-09-0002 D2015-12-0001 C2016-01-0001 D2015-12-0002 C2015-12-0002 D2015-12-0003 D2016-01-0002
Recalling firm:
Echopixel, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2016

Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift

The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88610
Lot/product code:
Acorn 130/180 Seat Squab, included as part of The Acorn 130 Straight Stairlift and the Acorn 180 Curved Stairlift. Serial Numbers: 140110386215,140110356934,140110330295,140110410265,140110356903,140110319711,140110353380,140110358263,140110387720,140110357449,140110348263,140110380857,140110357022,140110334193,140110390695,140110348564,140110364396,140110362060,140110278902,140110360364,140110263037,140110366547,140110320108,140110372638,140110387248,140110367036,140110311884,140110405234,140110387712,140110400646,140110378178,140110393130,140110389009,140110348935,140110409990,140110413893,140110392454,140110253282,140110406587,140110367992,140110370968,140110367770,140110308838,140110387501,140110402408,140110361497,140110366632,140110365928,140110352238,140110406996,140110401030,140110382733,140110361514,140110363598,140110382800,140110387432,140110367208,140110391181,140110374800,140110370938,140110399914,140110253288,140110355287,140110405166,140110301171,140110358373,140110286761,140110364341,140110399265,140110352528,140110358931,140110358946,140110362374,140110362380,140110366428,140110369259,140110369263,140110369271,140110369300,140110378184,140110378198,140110378199,140110378209,140110382307,140110382320,140110382353,140110399571,140110399585,140110399595,140110402205,140110410470,140110413890,140110413896,140110413899,140110361487,140110361821,140110361829,140110361833,140110361839,140110363852,140110363880,140110363562,140110363564,140110363568,140110363569,140110363577,140110366995,140110367005,140110367011,140110367024,140110367026,140110367027,140110367028,140110370953,140110370955,140110368536,140110368595,140110368596,140110368622,140110378228,140110378246,140110385961,140110385967,140110385978,140110385981,140110385982,140110385983,140110386327,140110386333,140110386335,140110386339,140110386341,140110386346,140110386512,140110386518,140110386522,140110386535,140110388078,140110388069,140110388213,140110388226,140110388232,140110391105,140110390744,140110390745,140110390761,140110390762,140110390763,140110390765,140110390774,140110392504,140110392535,140110392544,140110392549,140110395496,140110399232,140110399233,140110399234,140110399240,140110399241,140110399242,140110399244,140110399247,140110399248,140110399249,140110399253,140110399254,140110399275,140110399611,140110399617,140110399620,140110399635,140110401637,140110401642,140110401649,140110401654,140110401660,140110401661,140110401666,140110401670,140110401671,140110407014,140110407015,140110407021,140110407022,140110407023,140110407026,140110407028,140110407030,140110407034,140110407039,140110407040,140110410275,140110410287,140110410288,140110410292,140110410298,140110410299,140110410304,140110410346,140110410349,140110409492,140110409652,140110412200,140110366621,140110353688,140110325996,140110364414,140110408994,140110372839,140110309210,140110409188,140110382424,140110359342,140110249011,140110278924,140110373685,140110378472,140110378484,140110387365,140110387375,140110388725,140110388194,140110388200,140110393569,140110399693,140110407106,140110407131,140110404870,140110383628,140110383643,140110383652,140110384609,140110384994,140110377424,140110383564,140110386447,140110386449,140110386458,140110386460,140110388084,140110357261,140110377102,140110377105,140110378298,140110378306,140110378310,140110403136,140110393722,140110303498,140110394367,140110396890,140110361572,140110361577,140110361580,140110361590,140110361606,140110362073,140110362140,140110362151,140110362152,140110362158,140110375027,140110375031,140110375044,140110395570,140110395576,140110395604,140110371426,140110377082,140110377092,140110377101,140110377114,140110377115,140110378297,140110378315,140110378325,140110378328,140110378331,140110360462,140110364754,140110378126,140110378538,140110378549,140110378574,140110393522,140110393557,140110401693,140110405131,140110405323,140110409007,140110409015,140110410111,140110410127,140110366971,140110370939,140110383478,140110386313,140110387306,140110267760,140110390089,140110262914,140110366988,140110386837,140110386839,140110324449,140110357161,140110357186,140110363732,140110369252,140110383578,140110383589,140110383603,140110383678,140110384539,140110372977,140110358492,140110364329,140110360418,140110360440,140110361019,140110353342,140110367248,140110379607,140110386020,140110385362,140110385838,140110385828,140110386176,140110386188,140110386508,140110386690,140110388203,140110392160,140110389468,140110399813,140110400708,140110400561,140110400572,140110400578,140110400579,140110402289,140110402796,140110405427,140110405438,140110405439,140110405441,140110405455,140110396039,140110366562,140110393302,140110409285,140110409319,140110409679,140110409752,140110369289,140110373302,140110385737,140110387841,140110387859,140110387867,140110368017,140110387543,140110393709,140110393993,140110382324,140110399774,140110401682,140110359416,140110360973,140110367172,140110383686,140110392109,140110392468,1401103… (truncated, 343702 characters total — see the official FDA record for the full value)
Recalling firm:
Acorn Stairlifts, Inc
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled May 26, 2016

Remeven Cream, (50% Urea in a Cream Base), a) 5.0 oz (142 g) and b) 9.0 oz (255 g) tubes, Rx only, Manufactured by Sonar Products Inc, Carlstadt, NJ. Distributed by Stratus Pharmaceuticals Inc., Miami, FL.

Crystallization; Complaints that cream appears to have crystallized

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-1464-2016
Lot/product code:
a) Lot (Exp): 8020 (02/17), 8096 (07/18), 8125 (08/18), 8169 (10/18). NDC 58980-680-50 b) Lot (Exp): 8020 (02/17), 8125 (08/18), 8170 (10/18). NDC 58980-680-90
Recalling firm:
Stratus Pharmaceuticals Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 15, 2016

EVA Floor Lifts, Model Numbers: 400, 450, 600

After feedback from customers and internal suspicion, Handicare has become aware that abnormal use of Eva-lifts could lead to a deterioation in the joint of the liftarm. This could lead to injury if the joint breaks. All lifts must therefore be checked and reported back to the manuafacturer.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
85362
Lot/product code:
All affected models
Recalling firm:
Handicare AB
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 22, 2016

Olympus Scientific Solutions Americas Corporation (OSSA) Model: Analytical X-Ray System X -Ray Fluorescence. Intended to emit ionizing radiation Delta with models: DC-2000, DC-4000, DC-6000, DI-2000, DP-2000, DP-4000, DP-4050, DP- 6000, DPO-4000, DPO-6000, DS-2000, DS-4000, DS-6000, DS-6500, Delta, Delta 50, Delta Classic Plus, Delta Element, Delta Premium , Delta Professional , and Delta-Pl us.

Trigger lock option does not always prevent x-ray generation. Specifically if the unit is in test mode or repeat test mode then the trigger lock may not prevent x-ray initiation when the trigger is pulled. The correction is via repair by a software update.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
74593
Lot/product code:
All Models of the Delta XRF Analyzer with Software version 2.5.17.1 and higher
Recalling firm:
Olympus Scientific Solutions Americas
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 28, 2016

TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a professional setting or by self-testing.

Product gives incorrect low blood glucose levels.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
74805
Lot/product code:
Strip Lot #: PS2265 PS2283 PS2285 PS2281 PS2278 PS2276 PS2275 PS2215 PS2271 PS2279 PS2209 PS2299 PS2273 PS2274 PS2280 PS2219 PS2277 PS2268 PS2282 PS2296 PS2288 PS2284 PS2291 PS2287 PS2286 PS2297 PS2252 PS2293 PS2302 PS2292 PS2313 PS2270 PS2190 PS2189 PS2290 PS2298 PS2303 PS2289 PS2294 PS2295 PS2300 PS2304 PS2325 PS2312 PS2311 PS2305 PS2306 PS2315 PS2301 PS2314 PS2310 PS2347 PS2309 PS2318 PS2395 PS2320 PS2321 PS2316 PS2317 PS2330 PS2327 PS2324 PS2323 PS2333 PS2326 PS2328 PS2334 PS2329 PS2331 PS2332 PS2336 PS2335 PS2340 PS2345 PS2308 PS2341 PS2339 PS2307 PS2343 PS2353 PS2352 PS2338 PS2348 PS2342 PS2355 PS2344 PS2359 PS2362 PS2357 PS2349 PS2376 PS2356 PS2350 PS2367 PS2351 PS2346 PS2354 PS2371 PS2360 PS2366 PS2364 PS2370 PS2355SER PS2363 PS2319 PS2365 PS2361 PS2368 PS2372 PS2381 PS2369 PS2377 PS2392 PS2380 PS2374 PS2375 PS2373 PS2378 PS2379 PS2382 PS2380SER PS2383 PS2389 PR2068 PS2393 PS2384 PS2400 PS2391 PS2401 PS2402 PS2408 PS2388 PS2386 PS2387 PS2390 PS2385 PS2399 PS2396 PS2406 PS2398 PS2409 PS2337 PS2397 PS2404 PS2403 PS2322 PS2412 PS2416 PS2417 PS2419 PS2418 PS2420 PS2405 PS2413 PS2414 PS2394 PS2411 PS2415 PS2421 PS2267INT PS2336ILA PS2190IGB PS2267IGB PR2122INT PS2189INT PS2319INT PS2252ILA PS2345INT PS2279ILA PS2319IGB PS2407IGB PS2322IGB PS2349ITT PS2394ILA PS2307ILA PS2309ILA PS2308ILA PS2415INT PS2351ILA PS2337ILA PS2415ILA PS2411ILA PS2384ILA PS2394INT PS2413ILA PR2156INT PS2284ICA PS2316ICA PS2335ICA RS4646 RS4631 RS4649 RS4645 RS4652 RS4641 RS4653 RS4638 RS4612 RS4644 RS4655 RS4669 RS4567 RS4639 RS4605 RS4659 RS4654 RS4657 RS4608 RS4660 RS4662 RS4634 RS4676 RS4670 RS4665 RS4544 RS4674 RS4607 RS4688 RS4673 RS4667 RS4678 RS4680 RS4686 RS4677 RS4679 RS4695 RS4699 RS4703 RS4689 RS4704 RS4692 RS4694 RS4698 RS4663 RS4705 RS4708 RS4719 RS4710 RS4715 RS4717 RS4714 RS4723 RR4521 RS4716 RS4724 RS4645IGB RS4567ICA RS4704ICA DR4559 DS4648 DS4624 DS4658 DS4579 DS4672 DR4559IBR DR4559INT DS4624INT DS4648IBR DS4658INT DS4658IBR DS4624IBR DS4579IBR DS4711INT DS4672INT BS4643 BS4640 BS4650 BS4668 BS4661 BS4588 BS4651 BS4621 BS4664 BS4615 BS4675 BS4666 BS4629 BS4687 BS4681 BS4696 BS4700 BS4707 BS4693 BS4671 BS4690 BS4697 BS4701 BS4706 BS4709 BS4713 BS4720 BS4682 BS4683 BS4721 BS4643INT BS4588INT BS4697INT BS4651INT BS4629INT BS4682IAT BS4629IAT BS4602INT BS4666INT BS4682INT BS4603INT BS4671IAT. Kit Lot #: KS0967 KS1022 KS1214 KS1312 KS1154 KS1688 KS1631 KS1301 ks1133 KS1341 KS1063 KS1109 KS0968 ks1449 KS1340 KS1032 KS1266 KS1714 KS1910 KS1473 KS1546 KS1524 KS1759 KS1152 ks1108 KS1153 KS1243 KS1790 KS1763 KS1132 KS1306 KS0981 ks1323 KS1175 KS1909 KS1426 KS1215 KS1687 KS1533 KS1300 KS1643 KS1360 KS1779 KS1671 KS1933 KS1943 KS1597 KS1020 KS1417 KS1488 KS1730 KS1732 KS1496 KS1650 KS1469 KS2235 KS1501 KS1736 KS1531 KS1107 KS1580 KS1021 KS1267 KS1051 KS1646 KS1483 KS1363 KS1925 KS1659 KS0994 KS1028 KS1369 KS1627 KS1049 KS1389 KS1701 KS1053 KS1048 KS1444 KS1176 KS1364 KS0980 KS1147 KS1797 KS1957 KS1459 KS1497 KS1767 KS1311 S1700 S1700 KS1474 KS1276 KS1532 KS1792 KS1542 KS1366 KS1339 KS0988 KS1268 KS1445 ks1045 KS1447 KS1362 KS1545 KS1725 KS1692 ks1434 KS2217 KS1543 KS1031 KS1047 KS1295 KS2260 KS1764 KS1189 KS1726 KS1510 KS1278 KS2415 KS1258 KS1748 KS0996 KS1734 KS1121 KS1724 KS1187 KS1574 KS1422 KS2324 KS1365 KS1023 KS1594 KS1525 KS2373 KS1303 KS1448 KS2449 KS1534 ks1188 ks1443 KS1661 KS1930 KS2437 KS1230 KS0970ITH KS1423 KS1999ITH KS1418ITH KS1134ITH KS1229 KS1228 KS0818 KS1030ITH KS1419ITH KS1241 KS1941 KS1796 KS1954 KS1190 KS1281 KS1559 KS1489 KS1737 KS1927 KS1326 KS1560 KS1528 KS1000 KS1162 KS1453 KS1942 KS0993 KS1145 KS1944 KS1751 KS1320 KS0995 KS1441 KS1747 KS1277 KS1052 KS1599 KS1752 KS1217 KS1731 KS1013 KS1302 KS1553 KS1928 KS1186 KS1395 KS1144 KS1544 KS1487 KS1697 KS1940 KS1762 KS2414 KS1465 KS1917 KS2417 KS1468 KS1143 KS1089 KS2418 KS1116 KS1500 KS1006 KS1535 KS1704 KS1071 KS1288 KS1626 KS1628 KS2323 KS1070 KS1115 KS1446 KS0992 KS1573 KS0999 KS1705 KS1750 KS1221 KS1127 KS1567 KS1527 KS1557 KS2453 KS2971 KS1406 KS1680 KS1682 KS1056 KS1057 KS1679 KS1681 KS1684TI KS1683TI KS1786TI KS1298TI KS1042TI KS1526TI KS1988TI KS1297TI KS1787TI KS1036TI KS1041TI KS1604TI KS1177TI KS1432TI KS1603TI KS2051TI KS1135TI KS1130TI KS0921TIIBD KS1699TIIBD KS1347TI KS1348TI KS0910TI KS1346TI. Prepackaged Lot #: KS1236 KS0889 KS1670 KS1932 KS1456 KS1709 KS1250 KS1329 KS0896 KS1578 KS0948 KS1387 KS1648 ks1667 KS1736 KS1914 KS0900 KS1067 KS1665 KS0899 KS1076 KS1916 KS0946 KS1201 KS1582 KS1794 KS1197 KS1330 KS1294 KS0986 KS1309 KS1505 KS0975 KS1477 KS1262 KS1079 KS1458 KS1630 KS0891 KS1174 KS1203 KS1506 KS1663 KS1744 KS0850 KS1452TI KS1018TI KS1635TI KS1138TI KS0933TI KS1165TI KS1352TI KS1521TI KS1540TI KS1508TI KS1912TI KS1260TI KS1008TI KS0837TI KS1248TI KS1055TI KS1746TI KS1234TI KS1247TI KS0984TI KS1233TI KS1139TI KS1149TI KS1148TI.
Recalling firm:
Trividia Health
View official FDA record (opens in a new tab)